KRT9, keratin 9, 3857

N. diseases: 30; N. variants: 14
Disease: Congenital Camptodactyly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly 		0.010 Biomarker disease BEFREE We speculated that KRT9 plays a complicated role in the genesis of EPPK with knuckle pads and camptodactyly, which needs to be further investigated. 21715251 2012